Providing patient information, medical, and health advice. Interactive question and answer forums staffed by online doctors from leading medical centers. Extensive library of articles on all diseases and health conditions. Specializing in areas such as heart disease, neurology, child behavior, dermatology, mental health, gastroenterology, urology, respiratory disorders, addiction, family health, ...

National Organization for Rare Disorders is dedicated to helping people with rare, orphan diseases. Rarediseases.org contains information on the prevention, treatment and cure of rare diseases.

Our Silver Anniversary! Online Discussion/Support Groups: General Caregiving LGBT Caring Community Huntington's Disease & Movement Disorders Updated Fact Sheets: Alzheimer's Disease Early-Stage Alzheimer's Disease Nuevos Folletos Informativos en Espa ol Workshops and Events Proceedings from FCA's National Conference Released Latest Newsletter Clinical Trials & Research NCC Public Policy Briefs ...

RESNA is an interdisciplinary association for the advancement of rehabilitation and assistive technologies (AT).

The Global Fund to Fight AIDS, Tuberculosis and Malaria ...

Web site of the National Aphasia Association. Your Internet source for information and resources on the communication impairment APHASIA.

IFFGD addresses issues surrounding life with gastrointestinal (GI) disorders.

Home page of the Dystonia Medical Research Foundation. Links to pages on all aspects of the movement disorder dystonia (blepharospasm, spasmodic torticollis, spasmodic dysphonia, writer's cramp).

Office of Rare Diseases Skip Navigation Links Welcome to the website of the Office of Rare Diseases (ORD). Here you can find information on more than 6000 rare diseases, including current research, publications from scientific and medical journals, completed research, ongoing studies, and patient support groups. (URL: http://rarediseases.info.nih.gov/) The Office of Rare Diseases (ORD) is making ...

A not-for-profit organization serving children and adults with Down syndrome and their families in the Chicago metropolitan area.

The Hormone Foundation was established by The Endocrine Society to promote the prevention, diagnosis, and treatment of hormone-related conditions and diseases, such as menopause.

Dedicated to helping sufferers, who are living with IBS, manage their own health with IBS since 1987. This IBS Support Group website, an IBS Community, provides a bulletin board, access to resource lists, diagnosis, medical tests, treatment, books, meetings, studies and a list of medications.

Gaucher Disease is the most common lipid-storage disorder, and is the most common genetic disease affecting Jewish people of Eastern European ancestry. Gaucher Disease results from a specific enzyme deficiency in the body, caused by a genetic mutation received from both parents. The disease course is quite variable, ranging from no outward symptoms to severe disability and death. Fortunately, ...

A support organization for persons with Transverse Myelitis and their family members.

The Coeliac Society UK - one of the largest donation funded charities of its kind, supporting 45, 000 members who are living with Coeliac Disease, Dermatitis Herpetiformis and related conditions.

A disability organization and parent support group, providing peer support and resource information to parents of children and adults with disabilities in Georgia.

Search our Site: sitemap Contributor's Choice Member of the United Way unitedway.org This Page is best viewed in 800 x 600 using the latest version of: Netscape Communicator Internet Explorer Spring, 2002 What's New The NPF is very proud to announce our partnership with HopeLink. HopeLink has provided NPF with a free clinical trial service for Pancreatic Cancer patients. View our clinical trial ...

The International Pelvic Pain Society is a professional organization to enhance and improve the treatment of a variety of diseases that cause pelvic pain in women.

Home | our mission | message from mia | what's new | mia's heroes | about mia | bone marrow info girls in sports info | corporate support | photo gallery | donate online | foundation events | talk to us ...

Last updated: 10 June, 2002 These pages are designed for best viewing using 1024x768 screen resolution. We're very glad that you dropped by!!! Our Visit-O-Meter stands now at: (Since: 15 September 1995) Translate this page with InterTran (tm) Deutsch Francais Espa ol Portuguese Japanese (Shift JIS) Finnish Italiano Svensk Russian/ o ee (CP 1251) Nederlands Brasileiro Danske Islenska Norsk ...

EMS is a disease caused by taking the health food supplement l-tryptophan causing acute muscle and neurological pain ...

Information about Tourette Syndrome and TS-related links around the World , New Jersey TS Support Group Info, TS Discussion Forum, Guest Book; All guests interested in Tourette Syndrome are welcome.

A guide to Disfigurement Guidance and Skin Camouflage ...

This web site attempts to answer some of the most commonly-asked questions about cleft lip and palates ...

Please support the Brachial Plexus Palsy Foundation in it's efforts to help those who are affected by this injury and their families ...

The Melungeon Health Education and Support Network HELLO! I am Nancy Sparks Morrison, Co-author of the Sparks Genealogy Web Site at: http://SparksGenealogy.net This Melungeon Health Site is dedicated to the health of those Melungeons descendants who have one or more of the 5 major Mediterranean illnesses that are inherited through the Melungeon connection. I hope that you will find some answers ...

The MYOCLONUS RESEARCH FOUNDATION is a public charity, supporting research in myoclonus, investigating its basic mechanisms and developing new therapies. What is myoclonus What causes myoclonus How is myoclonus treated Self Help What is the Myoclonus Research Foundation Research support Video Tape Myoclonus Research Foundation 200 Old Palisade Road - Suite 17D Fort Lee, NJ 07024 E-Mail Us ...

An organization to furthering the understanding of diseases of the pituitary gland ...

The Acoustic Neuroma Association NSW Inc is a patient organised information and support group.

Friday, June 14, 2002 eMail Discussion Group! Enter your email address Subscribe UnSubscribe * This moderated email discussion group is limited to support topics only. eMail Fun group! Enter your email address Subscribe UnSubscribe * This is an un-moderated email discussion group Hello....My name is Lynn Brown and I live in Pell City, AL I am a Flight Attendant with clipped wings. I had my wings ...

Stiff-Man Syndrome information and ListServer ...

Those affected by Wolfram Syndrome have prepared this site to help other similarly affected families.This site contains information about the symptoms and challenges of Wolfram Syndrome.You may also contact other families with Wolfram Syndrome who are very happy to share their experiences with others who are affected by Wolfram Syndrome.